Kolor K, Lindsley D, Gallant J A
Department of Genetics, University of Washington, Seattle 98195.
J Mol Biol. 1993 Mar 5;230(1):1-5. doi: 10.1006/jmbi.1993.1118.
Previous work characterized ribosomal frameshifting within the sequence C UUC AAG provoked by lysyl-tRNA limitation. The ribosome frameshift is one base to the left of the AAG lysine codon, as shown by dotted overlining above. We now show that the frequency of this leftward ribosome frameshift is strongly influenced by the identity of the bases two, three and four positions to the left of the actual frameshift site. The nature of these influences coincides exactly with the possibilities of base-pairing between the sequence and the anticodon of the P-site peptidyl-tRNA when shifted one base to the left just upstream of the frameshift site. We conclude that a peptidyl shift in the P-site is intimately involved in leftward frameshifting in the adjacent A site when it codes for an aminoacyl-tRNA in short supply.
先前的研究对由赖氨酰 - tRNA限制引发的、在序列C UUC AAG内的核糖体移码进行了表征。核糖体移码发生在AAG赖氨酸密码子左侧一个碱基处,如上方虚线加下划线所示。我们现在表明,这种向左的核糖体移码频率受到实际移码位点左侧第二个、第三个和第四个碱基身份的强烈影响。这些影响的性质与移码位点上游一个碱基处向左移动时序列与P位点肽基 - tRNA反密码子之间碱基配对的可能性完全一致。我们得出结论,当P位点编码供应不足的氨酰 - tRNA时,P位点的肽基移位与相邻A位点的向左移码密切相关。